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A mild light-induced cleavage of the S–O bond of aryl sulfonate esters enables efficient sulfonylation of vinylarenes
A new mode of S–O bond activation has been discovered, which constitutes novel reactivity of easily available and bench-stable arylsulfonate phenol esters. This protocol enables access to putative sulfonyl radical intermediates, which enable straightforward access to valuable vinyl sulfones.
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148202/ https://www.ncbi.nlm.nih.gov/pubmed/30288238 http://dx.doi.org/10.1039/c8sc02769b |
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author | Ratushnyy, Maxim Kamenova, Monika Gevorgyan, Vladimir |
author_facet | Ratushnyy, Maxim Kamenova, Monika Gevorgyan, Vladimir |
author_sort | Ratushnyy, Maxim |
collection | PubMed |
description | A new mode of S–O bond activation has been discovered, which constitutes novel reactivity of easily available and bench-stable arylsulfonate phenol esters. This protocol enables access to putative sulfonyl radical intermediates, which enable straightforward access to valuable vinyl sulfones. |
format | Online Article Text |
id | pubmed-6148202 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-61482022018-10-04 A mild light-induced cleavage of the S–O bond of aryl sulfonate esters enables efficient sulfonylation of vinylarenes Ratushnyy, Maxim Kamenova, Monika Gevorgyan, Vladimir Chem Sci Chemistry A new mode of S–O bond activation has been discovered, which constitutes novel reactivity of easily available and bench-stable arylsulfonate phenol esters. This protocol enables access to putative sulfonyl radical intermediates, which enable straightforward access to valuable vinyl sulfones. Royal Society of Chemistry 2018-07-25 /pmc/articles/PMC6148202/ /pubmed/30288238 http://dx.doi.org/10.1039/c8sc02769b Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0) |
spellingShingle | Chemistry Ratushnyy, Maxim Kamenova, Monika Gevorgyan, Vladimir A mild light-induced cleavage of the S–O bond of aryl sulfonate esters enables efficient sulfonylation of vinylarenes |
title | A mild light-induced cleavage of the S–O bond of aryl sulfonate esters enables efficient sulfonylation of vinylarenes
|
title_full | A mild light-induced cleavage of the S–O bond of aryl sulfonate esters enables efficient sulfonylation of vinylarenes
|
title_fullStr | A mild light-induced cleavage of the S–O bond of aryl sulfonate esters enables efficient sulfonylation of vinylarenes
|
title_full_unstemmed | A mild light-induced cleavage of the S–O bond of aryl sulfonate esters enables efficient sulfonylation of vinylarenes
|
title_short | A mild light-induced cleavage of the S–O bond of aryl sulfonate esters enables efficient sulfonylation of vinylarenes
|
title_sort | mild light-induced cleavage of the s–o bond of aryl sulfonate esters enables efficient sulfonylation of vinylarenes |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148202/ https://www.ncbi.nlm.nih.gov/pubmed/30288238 http://dx.doi.org/10.1039/c8sc02769b |
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